Hydrochloric Acid → 4-(1-Propyl-piperidin-4-yl)-benzoic acid hydrochloride
반응식
C[O:2][C:3](=[O:19])[C:4]1[CH:9]=[CH:8][C:7]([CH:10]2[CH2:15][CH2:14][N:13]([CH2:16][CH2:17][CH3:18])[CH2:12][CH2:11]2)=[CH:6][CH:5]=1.[ClH:20]>>[ClH:20].[CH2:16]([N:13]1[CH2:12][CH2:11][CH:10]([C:7]2[CH:6]=[CH:5][C:4]([C:3]([OH:19])=[O:2])=[CH:9][CH:8]=2)[CH2:15][CH2:14]1)[CH2:17][CH3:18]참가 물질
3
반응 조건
- 온도
- 2 °C
실험 절차
4-(1-Propyl-piperidin-4-yl)-benzoic acid methyl ester (32 mmol) is dissolved in 4N HCl (45 ml) and heated under reflux for 7 hours. The mixture is cooled in an ice bath to 0-4° C. and the solid material formed is filtered off, washed with cold acetone and dried (vacuum). A brown powder with mp. >270° C., Rf=0.08 (CH2Cl2/MeOH=9:1) is obtained.
후처리
- temperatureheated
- temperatureunder reflux for 7 hours
- customthe solid material formed
- filtrationis filtered off
- washwashed with cold acetone
- customdried (vacuum)
- customA brown powder with mp. >270° C., Rf=0.08 (CH2Cl2/MeOH=9:1) is obtained
출처 및 근거
- ORD 기록
- ord-edfdd774c5724a3eb07fc43d78910dfe
- 출처 데이터셋
- uspto-grants-2003_11
- 특허 번호
- US06642239B2
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